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Mary M Jenkins

9PUBLICATIONS

35CO-AUTHORS

Epigenetics (incl. genome methylation and epigenomics)Gene mappingPharmacogenomicsNeurogeneticsDevelopmental genetics (incl. sex determination)

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Publications (9)

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|Apr 30, 2025

Exome Sequencing to Identify Novel Susceptibility Genes for Nonsyndromic Split-Hand/Ft Malformation: A Report From the National Birth Defects Prevention Study.

Tonia C Carter, Denise M Kay, Faith Pangilinan

|Jul 11, 2024

Exome sequencing identifies novel genes underlying primary congenital glaucoma in the National Birth Defects Prevention Study.

Elizabeth E Blue, Kristin J Moore, Kari E North

|May 16, 2024

Real-world data are not always big data: the case for primary data collection on medication use in pregnancy in the context of birth defects research.

Elizabeth C Ailes, Martha M Werler, Meredith M Howley

|Mar 21, 2023

Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child-parent trios and a case-control design to identify novel rare variants.

Pagna Sok, Aniko Sabo, Lynn M Almli

|Mar 11, 2022

Exome sequencing identifies variants in infants with sacral agenesis.

Georgia Pitsava, Marcia L Feldkamp, Nathan Pankratz

|Mar 08, 2021

Paternal genetic variants and risk of obstructive heart defects: A parent-of-origin approach.

Jenil Patel, Emine Bircan, Xinyu Tang

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Frequent Collaborators

6 joint publications

Gary M Shaw

6 joint publications

Paul A Romitti

5 joint publications

Andrew F Olshan

4 joint publications

Wendy N Nembhard

4 joint publications

Philip J Lupo

4 joint publications

Marcia L Feldkamp

4 joint publications

Marilyn L Browne

3 joint publications

Cynthia Moore

2 joint publications

Elizabeth E Blue

2 joint publications

A J Agopian

Frequent Collaborators

6 joint publications

Gary M Shaw

6 joint publications

Paul A Romitti

5 joint publications

Andrew F Olshan

4 joint publications

Wendy N Nembhard

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